CN104487509B - 水性粘合剂组合物 - Google Patents
水性粘合剂组合物 Download PDFInfo
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- CN104487509B CN104487509B CN201380039061.2A CN201380039061A CN104487509B CN 104487509 B CN104487509 B CN 104487509B CN 201380039061 A CN201380039061 A CN 201380039061A CN 104487509 B CN104487509 B CN 104487509B
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- 229910052725 zinc Inorganic materials 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/10—Homopolymers or copolymers of methacrylic acid esters
- C09D133/12—Homopolymers or copolymers of methyl methacrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
- C08F265/06—Polymerisation of acrylate or methacrylate esters on to polymers thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/10—Homopolymers or copolymers of methacrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/54—Aqueous solutions or dispersions
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2308/00—Chemical blending or stepwise polymerisation process with the same catalyst
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/003—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12169244.6 | 2012-05-24 | ||
| EP12169244 | 2012-05-24 | ||
| EP12191424.6 | 2012-11-06 | ||
| EP12191424 | 2012-11-06 | ||
| PCT/EP2013/060558 WO2013174894A1 (en) | 2012-05-24 | 2013-05-23 | Aqueous binder compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN104487509A CN104487509A (zh) | 2015-04-01 |
| CN104487509B true CN104487509B (zh) | 2016-05-04 |
Family
ID=48470993
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201380039061.2A Active CN104487509B (zh) | 2012-05-24 | 2013-05-23 | 水性粘合剂组合物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9382442B2 (ja) |
| EP (1) | EP2855579B1 (ja) |
| JP (1) | JP6275124B2 (ja) |
| CN (1) | CN104487509B (ja) |
| ES (1) | ES2571582T3 (ja) |
| PL (1) | PL2855579T3 (ja) |
| WO (1) | WO2013174894A1 (ja) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| ES2833098T3 (es) | 2013-02-22 | 2021-06-14 | Basf Se | Procedimiento para la producción de preparaciones de poliuretano acuosas |
| CN107112540B (zh) | 2014-11-18 | 2021-06-01 | 日本瑞翁株式会社 | 锂离子二次电池电极用粘结剂组合物 |
| EP3227346B1 (de) | 2014-12-03 | 2019-01-09 | Basf Se | Bindemittelsystem für hochglänzende anstriche |
| TWI705114B (zh) * | 2015-08-31 | 2020-09-21 | 美商羅門哈斯公司 | 用於皮革面塗層的水性多段共聚物組合物 |
| AU2015417100B2 (en) * | 2015-12-14 | 2020-09-03 | Dow Global Technologies Llc | Aqueous coating composition and process of making the same |
| WO2017214918A1 (en) * | 2016-06-16 | 2017-12-21 | Dow Global Technologies Llc | Aqueous polymer dispersion and aqueous coating composition comprising the same |
| EP3487895B1 (de) | 2016-07-20 | 2023-02-01 | Basf Se | Verfahren zur herstellung einer wässrigen polymerdispersion mit hoher chemikalienbeständigkeit |
| CN109563192B (zh) * | 2016-07-29 | 2021-09-28 | 巴斯夫欧洲公司 | 水性聚合物分散体 |
| US10662273B2 (en) | 2016-12-19 | 2020-05-26 | Celanese International Corporation | Waterborne acrylic dispersions with high biorenewable content |
| CN107189004A (zh) * | 2017-03-01 | 2017-09-22 | 长木（宁波）新材料科技有限公司 | 一种快速交联的水性塑胶用丙烯酸树脂的制备方法 |
| CN114539520B (zh) | 2018-02-08 | 2024-05-10 | 广东华润涂料有限公司 | 可uv固化的非异氰酸酯聚脲聚合物以及含有该聚合物的可uv固化涂料组合物 |
| CN116836345A (zh) * | 2018-02-27 | 2023-10-03 | 沃特世科技公司 | 具有梯度组成的聚合物颗粒及其生产方法 |
| JP7412776B2 (ja) | 2019-01-11 | 2024-01-15 | 学校法人 工学院大学 | 磁気支持装置 |
| US20220186431A1 (en) * | 2019-03-29 | 2022-06-16 | Toray Industries, Inc. | Sheet-shaped article and manufacturing method therefor |
| EP3822325A1 (en) * | 2019-11-14 | 2021-05-19 | PPG Europe B.V. | Coating composition and use thereof |
| AU2021231199A1 (en) * | 2020-03-06 | 2022-07-21 | Sika Technology Ag | Water-based dispersion floor adhesive with high dimensional stability |
| EP4172281A4 (en) * | 2020-06-28 | 2024-02-21 | Dow Global Technologies Llc | AQUEOUS DISPERSION OF MULTI-STAG POLYMER PARTICLES AND METHOD FOR THE PRODUCTION THEREOF |
| KR20230041759A (ko) * | 2020-07-20 | 2023-03-24 | 바스프 에스이 | 수계 코팅 조성물에서 결합제로서 적합한 필름-형성 공중합체의 수성 중합체 라텍스 |
| WO2023118439A1 (en) * | 2021-12-23 | 2023-06-29 | Basf Se | Use of polymer dispersions in waterborne coating formulations and polymer dispersions therefor |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0653461A2 (en) * | 1993-11-11 | 1995-05-17 | Kirin Beer Kabushiki Kaisha | Container composed of a saturated polyester resin composition |
| DE4442722A1 (de) * | 1994-12-01 | 1996-06-05 | Basf Ag | Schlagzäh thermoplastische Formmassen |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4977219A (en) | 1983-02-24 | 1990-12-11 | Union Carbide Chemicals And Plastics Company, Inc. | Low temperature crosslinking of water-borne resins |
| DE3512918A1 (de) | 1985-04-11 | 1986-10-16 | Bayer Ag, 5090 Leverkusen | Carbodiimidgruppen enthaltende isocyanat-derivate, ein verfahren zu ihrer herstellung und ihre verwendung als zusatzmittel fuer waessrige loesungen oder dispersionen von kunststoffen |
| US4820863A (en) | 1986-03-31 | 1989-04-11 | Union Carbide Corporation | Surface active polycarbodiimides |
| JPS63172718A (ja) | 1986-12-30 | 1988-07-16 | ユニオン・カーバイド・コーポレーション | 表面活性ポリカルボジイミド |
| DE3720860A1 (de) | 1987-06-24 | 1989-01-05 | Basf Ag | Lagerstabile waessrige polymerdispersionen |
| US5117059A (en) | 1989-06-01 | 1992-05-26 | Union Carbide Chemicals & Plastics Technology Corporation | Monodisperse multifunctional carbodiimides |
| US5104928A (en) * | 1990-01-12 | 1992-04-14 | The Glidden Company | Thermosetting coatings containing carbodiimides |
| US5066705A (en) * | 1990-01-17 | 1991-11-19 | The Glidden Company | Ambient cure protective coatings for plastic substrates |
| US5008363A (en) | 1990-03-23 | 1991-04-16 | Union Carbide Chemicals And Plastics Technology Corporation | Low temperature active aliphatic aromatic polycarbodiimides |
| NL9100578A (nl) | 1991-04-03 | 1992-11-02 | Stahl Holland Bv | Multifunctionele waterdispergeerbare verknopingsmiddelen. |
| US5352400A (en) | 1992-04-29 | 1994-10-04 | E. I. Du Pont De Nemours And Company | Carbodiimides and processes therefor |
| US5574083A (en) | 1993-06-11 | 1996-11-12 | Rohm And Haas Company | Aromatic polycarbodiimide crosslinkers |
| JP3629041B2 (ja) | 1994-06-10 | 2005-03-16 | 日清紡績株式会社 | 水性テトラメチルキシリレンカルボジイミド |
| US5936043A (en) | 1995-12-22 | 1999-08-10 | Rohm And Haas Company | Polymers crosslinkable with aliphatic polycarbodiimides |
| JP3518149B2 (ja) | 1996-02-29 | 2004-04-12 | 日清紡績株式会社 | 水性プレコートメタル用塗料 |
| JP3630527B2 (ja) | 1997-05-16 | 2005-03-16 | 日清紡績株式会社 | カルボジイミド系架橋剤及びその製造方法並びにコーティング材 |
| US6121406A (en) | 1998-04-20 | 2000-09-19 | Nisshinbo Industries, Inc. | Mixture of hydrophilic dicyclohexylmethanecarbodiimide |
| DE19820302A1 (de) * | 1998-05-04 | 2000-02-24 | Basf Ag | Kern/Schale-Partikel, ihre Herstellung und Verwendung |
| DE19821666A1 (de) | 1998-05-14 | 1999-11-25 | Basf Ag | Carbodiimide auf der Basis von 1,3-Bis-(1-methyl-1-isocyanatoethyl)-benzol |
| JP4278265B2 (ja) | 1999-04-30 | 2009-06-10 | 日本ペイント株式会社 | 熱硬化性水性塗料組成物およびこれを用いた塗膜形成方法、ならびに、複層塗膜形成方法 |
| US8076445B2 (en) * | 2000-01-11 | 2011-12-13 | Robert Shane Porzio | Oligocarbodiimides for the formation of crosslinked latex films |
| US6875834B2 (en) | 2001-01-30 | 2005-04-05 | Rohm And Haas Company | Two-component coating composition and method of preparation |
| DE10145344A1 (de) | 2001-09-14 | 2003-04-24 | Audi Ag | Verfahren zur Herstellung einer mehrschichtigen Lackierung einer Fahrzeugkarosserie und Beschichtungsmaterial |
| US7115682B2 (en) | 2002-09-26 | 2006-10-03 | Cytec Surface Specialties, Inc. | Removable, water-whitening resistant pressure sensitive adhesives |
| NL1023817C2 (nl) | 2003-07-03 | 2005-01-04 | Stahl Int Bv | Werkwijze voor de bereiding van stabiele polycarbodiimide dispersies in water, welke geen organische oplosmiddelen bevatten en als vernettingsmiddel kunnen worden gebruikt. |
| DE102004063380A1 (de) | 2004-12-23 | 2006-07-06 | Basf Ag | Verfahren zur Kaschierung unter Verwendung spezieller Vernetzer mit Carbodiimid-gruppen |
| NL1031053C2 (nl) | 2006-02-02 | 2007-08-03 | Stahl Int Bv | Werkwijze voor de bereiding van dispersies van vernettingsmiddelen in water. |
| JP5043912B2 (ja) * | 2009-10-08 | 2012-10-10 | 三菱レイヨン株式会社 | 水性被覆組成物 |
| US8900667B2 (en) | 2009-12-18 | 2014-12-02 | Ppg Industries Ohio, Inc. | One-component, ambient curable waterborne coating compositions, related methods and coated substrates |
| MX2012010068A (es) | 2010-03-02 | 2012-12-17 | Ppg Ind Ohio Inc | Composiciones de revestimiento de un componente, curables al ambiente, que cotienen agua, metodos relacionados y sustratos revestidos. |
| EP2371870B1 (en) | 2010-04-01 | 2012-07-11 | Rohm and Haas Company | Multistage emulsion polymer and coatings formed therefrom |
-
2013
- 2013-05-23 JP JP2015513169A patent/JP6275124B2/ja active Active
- 2013-05-23 US US14/400,594 patent/US9382442B2/en active Active
- 2013-05-23 ES ES13724276T patent/ES2571582T3/es active Active
- 2013-05-23 PL PL13724276.4T patent/PL2855579T3/pl unknown
- 2013-05-23 EP EP13724276.4A patent/EP2855579B1/en active Active
- 2013-05-23 CN CN201380039061.2A patent/CN104487509B/zh active Active
- 2013-05-23 WO PCT/EP2013/060558 patent/WO2013174894A1/en active Application Filing
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0653461A2 (en) * | 1993-11-11 | 1995-05-17 | Kirin Beer Kabushiki Kaisha | Container composed of a saturated polyester resin composition |
| DE4442722A1 (de) * | 1994-12-01 | 1996-06-05 | Basf Ag | Schlagzäh thermoplastische Formmassen |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2855579B1 (en) | 2016-03-16 |
| WO2013174894A1 (en) | 2013-11-28 |
| EP2855579A1 (en) | 2015-04-08 |
| PL2855579T3 (pl) | 2016-09-30 |
| ES2571582T3 (es) | 2016-05-26 |
| JP2015523429A (ja) | 2015-08-13 |
| CN104487509A (zh) | 2015-04-01 |
| US20150099843A1 (en) | 2015-04-09 |
| JP6275124B2 (ja) | 2018-02-07 |
| US9382442B2 (en) | 2016-07-05 |
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